ClinVar Miner

Submissions for variant NM_006662.3(SRCAP):c.3484C>T (p.Pro1162Ser)

gnomAD frequency: 0.00001  dbSNP: rs753700157
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000299649 SCV000332302 uncertain significance not provided 2015-06-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000299649 SCV003781973 likely benign not provided 2022-07-20 criteria provided, single submitter clinical testing

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